Sl. Sheng et al., beta-amyloid and its binding protein in the hippocampus of diabetic mice: effect of APP17 peptide, NEUROREPORT, 12(15), 2001, pp. 3317-3319
The objective of this study was to investigate whether changes in A beta an
d ERAB exist in the brain of diabetic mice, and to observe the effects of A
PP17 peptide. The numbers of neurons stained by APP17 peptide A beta1-40 A
beta1-42 A beta1-16 and ERAB antibodies in the brain of diabetic mice was i
ncreased compared with normal mice. Staining in APP17 peptide-protected mic
e was similar to normal mice. We conclude that increased A beta1-42 and ERA
B is an important cause of neuronal degeneration in diabetic encephalopathy
. APP17 peptide retards neuronal degeneration by regulating the metabolism
of A beta. NeuroReport 12:3317-3319 (C) 2001 Lippincott Williams & Wilkins.